Symbyax - 0002-3231-07 - (Olanzapine and Fluoxetine hydrochloride)

Alphabetical Index


Drug Information of Symbyax

Product NDC: 0002-3231
Proprietary Name: Symbyax
Non Proprietary Name: Olanzapine and Fluoxetine hydrochloride
Active Ingredient(s): 25; 6    mg/1; mg/1 & nbsp;   Olanzapine and Fluoxetine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Symbyax

Product NDC: 0002-3231
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021520
Marketing Category: NDA
Start Marketing Date: 20040119

Package Information of Symbyax

Package NDC: 0002-3231-07
Package Description: 7 CAPSULE in 1 BOTTLE (0002-3231-07)

NDC Information of Symbyax

NDC Code 0002-3231-07
Proprietary Name Symbyax
Package Description 7 CAPSULE in 1 BOTTLE (0002-3231-07)
Product NDC 0002-3231
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine and Fluoxetine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20040119
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name FLUOXETINE HYDROCHLORIDE; OLANZAPINE
Strength Number 25; 6
Strength Unit mg/1; mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Symbyax


General Information